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1H-pyrazole-4-carboxaldehyde, 3,5-dimethyl-1-(2-propenyl)is a pyrazole derivative with the molecular formula C9H10N2O. It features a carboxaldehyde group, two methyl groups at the 3 and 5 positions on the pyrazole ring, and a 2-propenyl group attached to the carbon at position 1 of the pyrazole ring. This chemical compound is known for its versatile reactivity and functional groups, making it a valuable building block in organic synthesis.

1155595-91-7

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1155595-91-7 Usage

Uses

Used in Pharmaceutical Industry:
1H-pyrazole-4-carboxaldehyde, 3,5-dimethyl-1-(2-propenyl)is used as a building block in the synthesis of various pharmaceuticals. Its unique structure and functional groups contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
This pyrazole derivative is also utilized in the production of agrochemicals, where its reactivity and functional groups can be employed to create compounds with pesticidal or herbicidal properties, contributing to more effective crop protection.
Used in Fine Chemicals Industry:
1H-pyrazole-4-carboxaldehyde, 3,5-dimethyl-1-(2-propenyl)serves as an essential component in the synthesis of other fine chemicals, including specialty chemicals and advanced materials, due to its versatile chemical properties.
Used as a Research Tool:
In addition to its practical applications, 1H-pyrazole-4-carboxaldehyde, 3,5-dimethyl-1-(2-propenyl)- may exhibit biological activity and is used as a research tool in the development of new drugs and chemical compounds, aiding scientists in understanding its potential interactions and effects within biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 1155595-91-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,5,5,9 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1155595-91:
(9*1)+(8*1)+(7*5)+(6*5)+(5*5)+(4*9)+(3*5)+(2*9)+(1*1)=177
177 % 10 = 7
So 1155595-91-7 is a valid CAS Registry Number.

1155595-91-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dimethyl-1-prop-2-enylpyrazole-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 1-ALLYL-3,5-DIMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1155595-91-7 SDS

1155595-91-7Downstream Products

1155595-91-7Relevant academic research and scientific papers

2-(pyrazol-4-yl)-1,3-oxaselenolanes from pyrazole carbaldehydes and 2-selanyl-1-ethanol

Papernaya, Lyubov K.,Shatrova, Alexandra A.,Levanova, Ekaterina P.,Albanov, Alexandr I.,Klyba, Lyudmila V.,Rudyakova, Elena V.,Levkovskaya, Galina G.

, p. 5 - 11 (2015)

Pyrazole carbaldehydes react with 2-selanyl-1-ethanol at room temperature in the presence of trimethylchlorosilane followed by treatment C with triethyl amine to afford the corresponding 2-(pyrazol-4-yl)-1,3-oxaselenolanes. The structure of the novel compounds was confirmed by IR, 13 C, 1 H, 15N, and 77 Se NMR spectroscopy.this article online at wileyonlinelibrary.com.

Synthesis of heterocyclic compounds from 4-formylpyrazoles

Mortikov,Rodinovskaya,Fedorov,Shestopalov,Belyakov

, p. 443 - 456 (2015/02/02)

Formylation of pyrazole and 2,5-dimethylpyrazole gave a number of pyrazole-containing aldehydes, which can be used to obtain chromenes, tetrahydrochromenes, 1,4-dihydropyrano[2,3-c]pyrazoles, pyrano[3,2-c]chromenes, thiochromeno[4,3-b]pyrans, pyrano[3,2-c

Selenoacetalyzation of 4-formylpyrazoles in the presence of trimethylchlorosilane

Papernaya, Lyubov K.,Shatrova, Alexandra A.,Levanova, Ekaterina P.,Albanov, Alexandr I.,Klyba, Lyudmila V.,Rudyakova, Elena V.,Levkovskaya, Galina G.

, p. 466 - 475 (2013/12/04)

The reaction of 3,5-dimethyl-4-formylpyrazoles, bearing various substituents at N-1 atom, with propane-1,3-diselenol and 2-hydroxypropane-1,3- diselenol in the presence of Cyrillic capital letter teCyrillic capital letter emSCl proceeds without heating to

Fragmentation of pyrazolecarbaldehyde thio- and dithioacetals under electron impact and chemical ionization

Klyba,Papernaya,Sanzheeva,Shatrova,Rudyakova,Levkovskaya

body text, p. 1851 - 1858 (2012/03/11)

The mass spectra of 1-substituted 3,5-dimethyl-1H-pyrazole-4-carbaldehyde bis(2-hydroxyethyl) dithioacetals and thioacetals were studied for the first time. The main fragmentation pathways of their molecular ions generated under electron impact and chemic

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